Home NDC 10967-601 Mitchum Roll On
Product NDC 10967-601
11-digit product format 109670601
Labeler code 10967
Product ID 10967-601_2a96a5f2-3367-a964-e063-6394a90a0e30
Type HUMAN OTC DRUG
Nonproprietary name Aluminum Zirconium Tetrachlorohydrex Gly
Dosage form LIQUID
Route TOPICAL
Labeler Revlon Consumer Products Corp
Application M019
Marketing category OTC MONOGRAPH DRUG
Marketing start 2014-01-01
Substance ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Active strength .2 g/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Mitchum Roll On
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY .2 g/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 8O386558JE Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 10967-601-17 Mitchum Roll On 50 mL in 1 CONTAINER LIQUID 50 3 10967-601-34 Mitchum Roll On 100 mL in 1 CONTAINER LIQUID 100 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 10967-601 MITCHUM ROLL ON (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY) LIQUID [REVLON CONSUMER PRODUCTS CORP] 3 Current NDC, Legacy NDC, 2 package rows 20250101_5387efbb-23db-4cbd-a3a7-7a0d15ab4ada.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 70 of 73 · 1,450 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 10967-601-17 10967060117 50 mL in 1 CONTAINER (10967-601-17) 50 ml 2014-01-01 0000-00-00 No No Current 10967-601-34 10967060134 100 mL in 1 CONTAINER (10967-601-34) 100 ml 2014-01-01 0000-00-00 No No Current